関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Ethyl Bromide | HCID 6332 | — |
| 反応物 | N-(4-Acetyl-2-methylphenyl)methanesulfonamide | HCID 19873430 | — |
| 反応物 | N-[4-[2-(ethylheptylamino)ethyl]phenyl]methanesulfonamide | HCID 53740092 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | N,N-diethyl-N-heptyl-4-[(methylsulfonyl)amino]benzeneethanaminium bromide | HCID 19873396 | — |
反応手順
A stirred solution of N-[4-[2-(ethylheptylamino)ethyl]phenyl]methanesulfonamide as prepared in Example 3 (0.332 g, 0.975 mmol) in acetonitrile (3 ml) is treated with HOAc, (0.056 ml, 0.975 mmol) and ethyl bromide (0.73 ml, 9.75 mmol). The solution is refluxed for 1 day, treated with additional ethyl bromide (1 ml) and acetonitrile (3 ml) and refluxed for one additional day. The mixture is concentrated; the residue is mixed with a solution of NaHCO3 (160 mg) in water and extracted with Et2O. The extracts are washed with water, dried (MgSO4) and concentrated to give recovered starting material (0.15 g, identified by TLC). The aqueous layers are combined, made strongly basic with 1N KOH, saturated with potassium bromide and washed with CH2Cl2. The aqueous layer is then acidified with 48% hydrogen bromide and extracted with CH2Cl2. The extracts are washed with saturated potassium bromide, dried (NaSO4) and concentrated to give 0.15 g of N,N-diethyl-N-heptyl-4-[(methylsulfonyl)amino]benzeneethanaminium bromide. MS calc'd for C20H37N2O2S (M+): 369.2576. Found: 369.2585.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05155268 |
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| 出典データセット | uspto-grants-1992_10 |
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| ORD ID | ord-e6e6ab513b7f4085a6d7b165e9cd6194 |
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| 出典メモ | uspto-grants-1992_10 |
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